PHARMAFull-time
Safety Aggreg Report Coord Trainee - Fresher
BANGALORE (IN)HYBRIDPOSTED: 9/16/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE OVERVIEW
Entry-level pharmacovigilance opportunity for B.Pharm or M.Pharm graduates with internship experience. The role supports safety aggregate reporting activities within IQVIA's life sciences and healthcare services environment.
ROLE DEFINITION & RESPONSIBILITIES
- •Support safety aggregate reporting activities
- •Coordinate assigned pharmacovigilance reporting workflows
- •Assist with review and organization of safety information
- •Maintain accurate documentation and tracking records
- •Coordinate with relevant internal teams to support timely deliverables
- •Follow applicable pharmacovigilance processes, quality requirements and standard operating procedures
- •Escalate discrepancies or issues through appropriate channels
Reporting Hierarchy: Reports to a pharmacovigilance or safety operations team lead/manager; Team structure not specified in the source posting
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- B.Pharm or M.Pharm qualification
- Freshers with internship experience eligible
- No full-time work experience required
- Interest in pharmacovigilance and drug safety operations
PREFERRED QUALIFICATIONS
- •Internship exposure in pharmacovigilance or drug safety
- •Familiarity with safety reporting concepts or pharmacovigilance terminology
- •Strong documentation and communication skills
REQUIRED VERIFIED SKILLS
Pharmacovigilance
safety aggregate reporting
drug safety
safety reporting
pharmacovigilance documentation
quality processes
SOP compliance
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Health insurance, provident fund, paid leave, professional development and hybrid-work support
The source posting does not disclose salary or bonus/equity, so no compensation figures are provided. Compensation should be confirmed directly through the employer during the recruitment process.
ORGANIZATION CONTEXT & CULTURE
IQVIA is a global provider of clinical research services, commercial insights and healthcare intelligence for the life sciences and healthcare industries, focused on helping accelerate the development and commercialization of medical treatments.
TEAM SIZE: 10,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
Culture: Mission-driven environment focused on life sciences, healthcare intelligence and improving patient outcomes; emphasizes integrity and professionalism in hiring and operations.
EXPECTED CAREER ROADMAP
A trainee can build foundational pharmacovigilance experience and progress into Safety Associate, Pharmacovigilance Associate, Senior Safety Associate and safety operations or aggregate reporting specialist roles with relevant experience and training.
APPLICATION ADVISORY
Highlight B.Pharm/M.Pharm qualification and relevant internship experience; emphasize pharmacovigilance, drug-safety or safety-reporting exposure; demonstrate accuracy and documentation skills; tailor the resume to aggregate reporting and safety operations; apply before the stated September 17, 2026 deadline.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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